Canonical Allele Identifier: CA1619889823

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164426G= , CM000668.2:g.33164426G=	GRCh38
NC_000006.11:g.33132203G= , CM000668.1:g.33132203G=	GRCh37
NC_000006.10:g.33240181G=	NCBI36
NG_011589.1:g.33043C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.717C=
ENST00000341947.7:c.4911C= MANE Select	ENSP00000339915.2:p.Leu1637=
ENST00000341947.6:c.4911C=	ENSP00000339915.2:p.Leu1637=
ENST00000361917.5:c.4590C=	ENSP00000355123.1:p.Leu1530=
ENST00000374708.8:c.4653C=	ENSP00000363840.4:p.Leu1551=
ENST00000477772.1:n.701C=
NM_080679.2:c.4590C=	NP_542410.2:p.Leu1530=
NM_080680.2:c.4911C=	NP_542411.2:p.Leu1637=
NM_080681.2:c.4653C=	NP_542412.2:p.Leu1551=
XM_011514298.1:c.4065C=	XP_011512600.1:p.Leu1355=
XM_011514299.1:c.4197C=	XP_011512601.1:p.Leu1399=
XM_011514300.1:c.4017C=	XP_011512602.1:p.Leu1339=
XM_011514301.1:c.3954C=	XP_011512603.1:p.Leu1318=
XM_011514302.1:c.3798C=	XP_011512604.1:p.Leu1266=
XM_011514299.2:c.4197C=	XP_011512601.1:p.Leu1399=
XM_011514300.2:c.4017C=	XP_011512602.1:p.Leu1339=
XM_011514302.2:c.3798C=	XP_011512604.1:p.Leu1266=
XM_017010250.1:c.4911C=	XP_016865739.1:p.Leu1637=
XM_017010251.2:c.3729C=	XP_016865740.1:p.Leu1243=
NM_080680.3:c.4911C= MANE Select	NP_542411.2:p.Leu1637=
NM_080681.3:c.4653C=	NP_542412.2:p.Leu1551=
NM_080679.3:c.4590C=	NP_542410.2:p.Leu1530=